Canonical Allele Identifier: CA2666624040
Gene: GBE1 HGNC NCBI

Linked Data

gnomAD v4: 3-81648759-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648759T>C , CM000665.2:g.81648759T>C GRCh38
NC_000003.11:g.81697910T>C , CM000665.1:g.81697910T>C GRCh37
NC_000003.10:g.81780600T>C NCBI36
NG_011810.1:g.118042A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.691+97A>G MANE Select ENSP00000410833.2:n.691+97A>G
ENST00000429644.6:c.691+97A>G ENSP00000410833.2:n.691+97A>G
ENST00000489715.1:c.568+97A>G ENSP00000419638.1:n.568+97A>G
ENST00000498468.1:n.219+97A>G
NM_000158.3:c.691+97A>G NP_000149.3:n.691+97A>G
NM_000158.4:c.691+97A>G MANE Select NP_000149.4:n.691+97A>G